SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs6275227 | snp | C/T | 0.290657 | 0.246672 | intron-variant | Rnf32 | Mm_Celera | 5:29200798 | ACAATAGGATTCACT[C/T]CACCTACAACAATAC | 56874 |
rs6275807 | snp | A/G | 0.290657 | 0.246672 | intron-variant | Rnf32 | Mm_Celera | 5:29200895 | AGAGGCCCTGAGTCC[A/G]ATGGCTCTAGGCTCA | 56874 |
rs6367864 | snp | A/G | 0.5 | 0 | intron-variant | Rnf32 | Mm_Celera | 5:29206442 | CATTAggggctagag[A/G]gatggtttggtgggt | 56874 |
rs33607723 | snp | C/T | 0.244898 | 0.249948 | upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29195043 | TGCCAAGAAAAAAAT[C/T]TGTAACTTTTAAGTG | 56874 |
rs45690633 | snp | C/T | 0.32 | 0.24 | synonymous-codon, nc-transcript-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29198009 | TCCTGATACAGCATG[C/T]TAAGAAATAAGGTAC | 56874 |
rs45818707 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29205325 | TTTAAGTTTAGGAGT[A/G]TAATTTAGCTAAGCA | 56874 |
rs46045216 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29200633 | TTACTTTTGATTACA[A/C]GTTCAGAATGGCCAG | 56874 |
rs46075957 | snp | C/T | 0.260355 | 0.249785 | intron-variant, downstream-variant-500B | Rnf32, Gm7420 | Mm_Celera | 5:29218956 | GCTCTATGACAAATG[C/T]TCTGATTCCTAGTGC | 56874 |
rs46184368 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29204489 | TGGCAGAGTGTAAAT[A/G]TCCTCACTTGTGTAA | 56874 |
rs46260216 | snp | G/T | | | intron-variant | Rnf32 | Mm_Celera | 5:29214063 | TGATCCTCATGGTGG[G/T]ACACTGACTGTTAAA | 56874 |
rs46266170 | snp | A/G | 0.336735 | 0.234472 | intron-variant | Rnf32 | Mm_Celera | 5:29221881 | GCACTATTACCACCC[A/G]CCTGAGCATTTCTGC | 56874 |
rs46271528 | snp | A/C | 0.142012 | 0.225474 | intron-variant, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29196292 | GGACCAGATTTCCAA[A/C]GACTTCTCTTGTCTC | 56874 |
rs46328199 | snp | A/T | 0.18 | 0.24 | utr-variant-3-prime, nc-transcript-variant | Rnf32 | Mm_Celera | 5:29225427 | TATATAGAGGAAATA[A/T]AAGTTCCTATTTAAC | 56874 |
rs46445471 | snp | C/T | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195678 | CTCCAAAGAGCCGCA[C/T]GGGTCAGCGCATCCT | 56874 |
rs46450594 | snp | C/T | 0.336735 | 0.234472 | intron-variant, upstream-variant-2KB | Rnf32, Gm7420 | Mm_Celera | 5:29215917 | TGAGTCTTGATTAGC[C/T]TCTCTCCGGGATAGA | 56874 |
rs46466150 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29201191 | AAGGTTGGGGCTACC[A/G]TGTGGGAAGTGACTG | 56874 |
rs46472957 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29212313 | CTCTGCTCCAGCTAA[A/G]GTCCAGACCATTGTT | 56874 |
rs46509173 | snp | C/T | 0.18 | 0.24 | intron-variant, upstream-variant-2KB | Rnf32, Gm7420 | Mm_Celera | 5:29216096 | ACTGAGAAGGAAAAG[C/T]GAATGAATACAAAGG | 56874 |
rs46546435 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29214127 | AGCCGCACACAAATG[A/G]TGTAAGCCCTTTTCT | 56874 |
rs46582462 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29222595 | TAAAACCTATTCAAC[C/T]TTGTAAACAAAACAG | 56874 |
rs46727087 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29205905 | TCAAAGCTGCCGACA[A/G]CACACTTCCTGCTGG | 56874 |
rs46754231 | snp | G/T | 0.152778 | 0.230321 | intron-variant, upstream-variant-2KB | Rnf32, Gm7420 | Mm_Celera | 5:29216672 | ACTTGGTCTGCTCTG[G/T]CCTGTGACTTCAGCC | 56874 |
rs46781931 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29221542 | TGGGCATATTGGGAG[A/G]GAAAAATTAAATTTA | 56874 |
rs46808250 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29221689 | GGCTTGTAAAAGTAC[A/G]CCATGTGCTGCTTTG | 56874 |
rs46845080 | snp | A/C | 0.18 | 0.24 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195280 | AGAAAAATCAATACA[A/C]TATTTCTGCTTGGCA | 56874 |
rs46847321 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B | Rnf32 | Mm_Celera | 5:29225689 | TAGGTAAATCAAATG[C/T]TAATGGTGGTGTTGC | 56874 |
rs46939235 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29205296 | CTCATAATTATGTTA[C/T]AGTAAGCTACAATTT | 56874 |
rs46990441 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29202195 | CATGGCTACTCAGCT[C/T]TTAGTATTAGACATC | 56874 |
rs47032561 | snp | A/T | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29222412 | AGTTTATATTTGAAC[A/T]TCTGTCCAGAGGTAA | 56874 |
rs47254754 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29221719 | GCAATTCTTTCCCAG[A/G]CTTTTCTCATATGAT | 56874 |
rs47393603 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195420 | AGGCCAGGAGCCGCA[A/G]GGACACCTCTCTCCA | 56874 |
rs47422727 | snp | A/T | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29194975 | AACAGTTGGCCTGCT[A/T]TTAATCTGCTTCTAC | 56874 |
rs47482928 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29211544 | CTAATCTGCTGGAGA[A/G]CAGGCACTCTAGATC | 56874 |
rs47512679 | snp | A/G | 0.132653 | 0.220748 | downstream-variant-500B | Rnf32 | Mm_Celera | 5:29225720 | AGATTCCTATGGTCC[A/G]TATAAGAGAATGAAA | 56874 |
rs47564299 | snp | C/T | 0.124444 | 0.216185 | synonymous-codon, nc-transcript-variant, missense | Rnf32 | Mm_Celera | 5:29205689 | GCTTTCCTGCTCACA[C/T]GTATTCCATAGGGTG | 56874 |
rs47592374 | snp | C/T | 0.152778 | 0.230321 | intron-variant | Rnf32 | Mm_Celera | 5:29214734 | GTAACAGCCATAATA[C/T]ATAAGCAGTGCCAAC | 56874 |
rs47638180 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29202625 | TGGGGCACTCATAAA[C/T]TCAATTAAGGAATGT | 56874 |
rs47644371 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29206031 | TTTCATGAGGAAGGT[C/G]TTAACATCTGATGAA | 56874 |
rs47648447 | snp | A/G | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29203696 | CCCAGCACAAATCCA[A/G]GCTTGGGTCCCCCAG | 56874 |
rs47678768 | snp | C/T | 0.260355 | 0.249785 | intron-variant | Rnf32 | Mm_Celera | 5:29214355 | AAAGGTGACACTACT[C/T]TGTCTGACAGTAAGT | 56874 |
rs47728870 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29201077 | GAGGCATGTCATGTG[C/T]ATCTGGAGACTTTAT | 56874 |
rs47734830 | snp | C/T | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197594 | CCAAAACACAAACAG[C/T]ATGCTGCTTTCCTGG | 56874 |
rs47810731 | snp | C/G | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195889 | ATGTAAGCGCGGGCG[C/G]AGCCAGCCGCTCGCA | 56874 |
rs47867505 | snp | A/T | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29202169 | TATTCCCATATTGAC[A/T]CTAGTGCTCTCATGG | 56874 |
rs47897790 | snp | A/G | | | intron-variant | Rnf32 | Mm_Celera | 5:29214064 | GATCCTCATGGTGGG[A/G]CACTGACTGTTAAAT | 56874 |
rs47925022 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29224080 | TCAGGAAGGACTGCC[C/T]TCATTCAGACGCTCC | 56874 |
rs47941753 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29200505 | GTGTGCAGGGGTCAG[A/T]GACAGGACACAGTGG | 56874 |
rs47948263 | snp | C/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29206865 | TGAGTGACCATCTGA[C/G]ACTGGTGAAGCTACA | 56874 |
rs48020081 | snp | A/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29196978 | CTGCCCTAGGCTTCT[A/G]AAGGGTCTGAACAGC | 56874 |
rs48045003 | snp | C/T | 0.297521 | 0.245442 | intron-variant, downstream-variant-500B | Rnf32, Gm7420 | Mm_Celera | 5:29218963 | GACAAATGTTCTGAT[C/T]CCTAGTGCCAAAGGT | 56874 |
rs48097658 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29221332 | TGATGGCCGTGAATG[A/T]GCTCCCTCTCCTACC | 56874 |
rs48107539 | snp | C/T | 0.124444 | 0.216185 | downstream-variant-500B | Rnf32 | GRCm38.p3 | 5:29225754 | TCATATATGGACCAA[C/T]GGAAAATCCCTGAAG | 56874 |
rs48131290 | snp | A/G | 0.142012 | 0.225474 | utr-variant-5-prime, intron-variant, nc-transcript-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29196089 | GTTCAGAAAAGGTGC[A/G]GCTGAGGGACAGGAA | 56874 |
rs48167685 | snp | A/T | 0.142012 | 0.225474 | intron-variant | Rnf32 | Mm_Celera | 5:29204957 | CGCTCTATTCTAAAA[A/T]TCCTTCCCTTAGTCC | 56874 |
rs48224000 | snp | A/C | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29200699 | CACTGATGTTCACCA[A/C]AAAAGCCTTTTCTCA | 56874 |
rs48303419 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29204940 | AAGGTTTTAGGTTTA[C/T]ACGCTCTATTCTAAA | 56874 |
rs48310030 | snp | C/T | 0.132653 | 0.220748 | intron-variant, upstream-variant-2KB | Rnf32, Gm7420 | Mm_Celera | 5:29216031 | AGTGGGAGTGTCTCA[C/T]AGAAATCACAAATGG | 56874 |
rs48400339 | snp | C/T | 0.244898 | 0.249948 | intron-variant | Rnf32 | Mm_Celera | 5:29219202 | ATAGATGCAATGCAT[C/T]GTATAGCTACAGTTT | 56874 |
rs48499034 | snp | G/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29203012 | AATGTGACTACATAT[G/T]CTAACATACATGAGG | 56874 |
rs48513836 | snp | C/T | 0.32 | 0.24 | synonymous-codon, intron-variant | Rnf32 | Mm_Celera | 5:29203071 | CCAGAAACTAGGCCT[C/T]TTGCCACCTCCCCCG | 56874 |
rs48593263 | snp | C/T | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29196898 | AAGGAATACTGCATA[C/T]AAACTTCTCTCATAG | 56874 |
rs48637406 | snp | G/T | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29195118 | ATTTATAATGACTTT[G/T]GGGACTTCTTAGTGA | 56874 |
rs48776174 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197815 | GATTGGGTTAGGACT[A/G]TGTAAATTAGACAGG | 56874 |
rs48815809 | snp | C/G | 0.152778 | 0.230321 | intron-variant | Rnf32 | Mm_Celera | 5:29212050 | GAGTGTTGGACCTGT[C/G]TGGCTGATACAGTAG | 56874 |
rs48865884 | snp | A/C | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29200534 | GGGAGGCCTGCACAG[A/C]ATGGAGAGGAAACTC | 56874 |
rs48962276 | snp | A/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29206359 | AGCTCAGGATGTGAT[A/T]ACTAACTCAGAGGAG | 56874 |
rs49044317 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29222373 | AAGATGCTGTGTGAA[A/G]TGGTACCATCCTGTT | 56874 |
rs49062352 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29224607 | CAGCTTAAAACATAA[A/G]ATTGGGAAGGTTTTA | 56874 |
rs49094556 | snp | A/G | 0.231111 | 0.249285 | intron-variant, nc-transcript-variant | Rnf32, Gm7420 | Mm_Celera | 5:29218340 | CTGAAATTCTCACCA[A/G]TCACCCAGATGCACC | 56874 |
rs49117710 | snp | A/G | 0.21875 | 0.248039 | intron-variant, nc-transcript-variant | Rnf32, Gm7420 | Mm_Celera | 5:29218443 | ACCTGTAGATGAGAA[A/G]AGCCTTGCTTTATTA | 56874 |
rs49135508 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195361 | AAGGACAGCGCGGGG[A/G]TGCAGACTTAAGAGG | 56874 |
rs49156714 | snp | C/G | 0.142012 | 0.225474 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197123 | TGTATGCATGAATGC[C/G]TAAGCTGCTCTGTGA | 56874 |
rs49176810 | snp | A/G | 0.142012 | 0.225474 | upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29193884 | CCAGGATATAGGACT[A/G]TGTTACTGGACTCAA | 56874 |
rs49301032 | snp | C/G | 0.142012 | 0.225474 | intron-variant | Rnf32 | Mm_Celera | 5:29210606 | GTTTAGTAAATAGGA[C/G]GTGTGAATAACAATG | 56874 |
rs49338504 | snp | C/T | 0.391111 | 0.206368 | downstream-variant-500B | Rnf32 | Mm_Celera | 5:29225882 | ACCTCTGAACTATAA[C/T]GCCTAGCATAGTGTA | 56874 |
rs49338734 | snp | A/G | 0.152778 | 0.230321 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195230 | TTCCAGGTGAATTAT[A/G]TACAATTAAAGTACA | 56874 |
rs49346675 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197445 | AGAGATGCTTAAGTC[A/G]CTTGCCCAAAAAAAG | 56874 |
rs49358970 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29206905 | TGCAGCTCACTTCAC[C/T]CTCAAGCTCGCTTTG | 56874 |
rs49385084 | snp | A/G | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29200514 | GGTCAGTGACAGGAC[A/G]CAGTGGGAGGCCTGC | 56874 |
rs49426090 | snp | A/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29200754 | GCTATTGCAGACACA[A/T]GTCTGTTCAGTTCAG | 56874 |
rs49442730 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29207121 | ATTATCGAACTGTTT[C/T]CGTAGTTATTATCTT | 56874 |
rs49444753 | snp | C/T | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29198563 | AAGACCTCCTACTCC[C/T]ATGTTTTTAGGATCG | 56874 |
rs49465060 | snp | G/T | 0.142012 | 0.225474 | upstream-variant-2KB, utr-variant-5-prime | Rnf32 | Mm_Celera | 5:29195391 | GGGTAGGAGGCAATG[G/T]CTCAGAGTGCAGAAG | 56874 |
rs49468018 | snp | A/G | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29202112 | CAAACTTTGTTTCCC[A/G]GCAGATGCATGCAGA | 56874 |
rs49477781 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf32 | Mm_Celera | 5:29213632 | AGAGATGGATCAAGT[A/G]CTTCCCTAGATCTGT | 56874 |
rs49590742 | snp | A/G | 0.231111 | 0.249285 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29198434 | TTGGGCCTGGGATTT[A/G]CTCTGCTTAGGTACT | 56874 |
rs49656252 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29200395 | TACAATCTATTGTAA[A/G]TCTGAAATCATTTTA | 56874 |
rs49697715 | snp | C/T | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197505 | CCCCCATATTCTGTC[C/T]GCCTGTGTGTTGGCC | 56874 |
rs49744044 | snp | A/G | 0.152778 | 0.230321 | intron-variant | Rnf32 | Mm_Celera | 5:29214810 | ATGTAGGATCTTGAG[A/G]AAAGAGGCCTACAGT | 56874 |
rs49781480 | snp | A/G | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29215062 | GAACACCATGTCTGG[A/G]ATGCCCTCTTATATC | 56874 |
rs49809873 | snp | A/G | 0.124444 | 0.216185 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29198423 | TACCATAGATGTTGG[A/G]CCTGGGATTTGCTCT | 56874 |
rs49898542 | snp | C/T | 0.32 | 0.24 | intron-variant | Rnf32 | Mm_Celera | 5:29203839 | AGTACACTTTGATTC[C/T]TACTCTCCAAGAGGA | 56874 |
rs49942343 | snp | C/T | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29221903 | CATTTCTGCTGTGTA[C/T]TTGTTCTTAAAAACT | 56874 |
rs50353806 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29205775 | TTGAACCATGAGCCC[C/T]GTTTGTAATTAGAAA | 56874 |
rs50443197 | snp | A/G | 0.32 | 0.24 | intron-variant, upstream-variant-2KB | Rnf32 | Mm_Celera | 5:29197247 | CTGGTCCCAAAACTA[A/G]AAGGGTTAATACCCA | 56874 |
rs50466836 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29202709 | AGCAAGGCAGTGCTG[C/T]AGATTGACAGTTAAA | 56874 |
rs50473004 | snp | C/T | 0.132653 | 0.220748 | downstream-variant-500B | Rnf32 | Mm_Celera | 5:29225587 | AATGCATAAGAATCT[C/T]CCTTTTATTTTTGTA | 56874 |
rs50619323 | snp | C/T | 0.124444 | 0.216185 | intron-variant | Rnf32 | Mm_Celera | 5:29205648 | TCCTAACTAGGACTC[C/T]TGTTCTCTTCTGGTG | 56874 |
rs50661091 | snp | C/T | 0.231111 | 0.249285 | intron-variant | Rnf32 | Mm_Celera | 5:29223081 | TGGAGTCCAGTGGAT[C/T]CAGCAGCTCCTATTA | 56874 |
rs50788486 | snp | G/T | 0.132653 | 0.220748 | intron-variant | Rnf32 | Mm_Celera | 5:29220984 | TACAGGCTAGACACA[G/T]CTGACCAGGTGTTGG | 56874 |